LISC-322 Neuroscience. Visual Field Representation. Visual Field Representation. Visual Field Representation. Visual Field Representation

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1 LISC-3 Neuroscience THE VISUAL SYSTEM Central Visual Pathways Each eye sees a part of the visual space that defines its visual field. The s of both eyes overlap extensively to create a binocular. eye both eyes eye Martin Paré Assistant Professor Physiology & Psychology The total is the sum of the and hemifields and consists of a binocular zone and two monocular zones. Just like the is divided into two hemifields, the retina is divided in half, relative to the fovea, into a nasal and a temporal hemiretina. hemifield hemifield monocular zone monocular zone binocular zone The axons of ganglion cells exit the eyes via the optic nerve, partially cross at the optic chiasm, and form two optic tracts, so that the and hemifields reach the and hemispheres. Each optic tract looks at the opposite hemifield, combining inputs from the ipsilateral temporal hemiretina and the contralateral nasal hemiretina. same side opposite side optic nerve optic tract hemisphere optic chiasm optic nerve optic tract hemisphere

2 Central Projections of the Retina Pretectum & Pupillary Light Reflex The retina projects to four subcortical regions in the brain: ) Lateral Geniculate nucleus ) Superior Colliculus 3) Hypothahalamus 4) Pretectum The pretectum controls the action of the pupillary constrictor muscle via its projection to both Edinger-Westphal nuclei. Pretectum & Pupillary Light Reflex The pretectum bilateral projections to the Edinger-Westphal nuclei ensure that both eyes react to light: shining a light into each eye can elicit a direct and a consensual pupillary reflex. This light reflex tells us about one s visual pathways status. The Swinging Light Test Normal direct consensual The Swinging Light Test Pretectum & Pupillary Light Reflex Normal Defective Left Afferent Pupil Defect Defective

3 Pretectum & Pupillary Light Reflex Pretectum & Pupillary Light Reflex Left Efferent Pupil Defect Defective In summary, pupillary reflexes are clinically important because they indicate the functional state of the afferent and efferent pathways mediating them. The absence of pupillary reflexes in an unconscious patient is a symptom of damage to the pretectum. Central Projections of the Retina The retina projects to four subcortical regions in the brain: ) Lateral Geniculate nucleus ) Superior Colliculus 3) Hypothahalamus 4) Pretectum The Lateral Geniculate nucleus (LGN) in the thalamus is the major target of the retinal ganglion cells. It receives inputs from both eyes and relays these messages to the primary visual cortex via the optic radiation. The retinal Magno and Parvo ganglion cells respectively project to ventral magnocellular layers and 4 dorsal parvocellular layers of the. Retinal Inputs LGN Organization

4 Each of the six LGN layers receives inputs from either the ipsilateral or contralateral eye, i.e., the ganglion cells of the eye project to layer, 4 & 6 of the LGN, and the eye ganglion cells project to its layer, 3 & 5. same side opposite side Selective lesions of the parvocellular and magnocellular LGN layers alter specific visual functions. Parvocellular lesion Magnocellular lesion Lesions restricted to the parvocellular layers severely disrupt the processing of color, while lesions of the magnocellular layers leave color vision unaffected. Lesions restricted to the parvocellular layers severely disrupts the processing of fine detail, while lesions of the magnocellular layers leave fine detail vision unaffected. Contrast Spatial frequency (Hz) Low high Spatial Frequency

5 Lesions restricted to the magnocellular layers severely disrupt the detection of fast moving stimuli, while lesions of the parvocellular layers affect only slow motion vision. Lesions restricted to the magnocellular layers severely disrupt the detection of fast flickering stimuli, while lesions of the parvocellular layers affect only slow flickering vision. Temporal frequency (Hz) slow fast Temporal frequency (Hz) Low high Optic Radiation Parvocellular layers Chromatic vision High fine detail vision Slow motion vision Magnocellular layers Achromatic vision Low fine detail vision Fast motion vision The LGN projections reach the primary visual cortex through the optic radiation. Axons carrying information about the superior sweep around the lateral horn of the ventricle under the temporal lobe (Meyer s loop). Those carrying information about the inferior travel under the cortex of the parietal lobe. Optic Radiation Primary Visual Cortex The primary visual cortex (V) has a representation of the contralateral visual hemifield. The foveal region is mapped in its most posterior part, whereas the more peripheral regions are mapped in progressively more anterior parts. The upper is mapped below the calcarine fissure, the lower above.

6 Primary Visual Cortex Because of the high density of ganglion cells in the fovea, the visual cortex has an expanded representation of the fovea. The highway of visual information (retina-lgn-v) can be vulnerable to strokes and tumors. Because of the orderly organization of this central visual pathway, such lesions produce characteristic gaps in the. Relatively small deficits are called scotomas, while large ones are called anopsias. Deficits in vision resulting from a single lesion can either be homonymous or nonhomonymous, i.e., affecting the same or different parts of the two eyes. INTACT VISION Scotoma Nonhomonymous anopsia retina retina Both - and -eye s are normal. Homonymous anopsia Cut at level A Cut at level B retina retina retina retina A lesion of the optic nerve causes a total loss of vision in the eye; it also produces a afferent pupil deficit. A lesion of the optic chiasm causes a loss of vision in the temporal half of both s: bitemporal hemianopsia.

7 Cut at level C retina retina A lesion of the optic tract causes a complete loss of vision in the hemifield: contralateral hemianopsia. Cut at level D Cut at level E retina retina retina retina A lesion of the optic radiation just after the LGN also causes a loss of vision in the hemifield: contralateral hemianopsia. A lesion of the optic radiation specific to Meyer s loop causes a loss of vision in the upper quadrant of the hemifield. The same is true for lesions to the lower bank of the calcarine sulcus. Cut at level F Cut at level G retina retina retina retina A lesion of the parietal portion of the optic radiation causes a loss of vision in the lower quadrant of the hemifield. The same is true for lesions to the upper bank of the calcarine sulcus. A lesion of the visual cortex causes a complete loss of vision in the hemifield: contralateral hemianopsia.

8 Cut at levels G & G Cut at levels G & G retina retina retina retina A lesion of both visual cortices causes a complete blindness. Lesions to visual cortex are usually only partial and spare foveal vision, probably because the foveal representation is so extensive that a single lesion is unlikely to destroy it all. Visual System: Central Visual Pathways Monocular blindness Bitemporal hemianopsia Contralateral hemianopsia Quadrantic hemianopsia Foveal sparing Reference for this Lecture: Neuroscience, nd edition (00) by Purves et al., Chapter. Reference for next Lecture: Neuroscience, nd edition (00) by Purves et al., Chapter & 6. Lectures are posted: Office Time: Tuesday & Thursday (5:00-7:00) Botterell Hall, Room 438